99 related articles for article (PubMed ID: 3326892)
1. Isolated glucocorticoid deficiency.
Bianchi C; di Natale B; Trifirò G; Weber G
J Endocrinol Invest; 1987 Dec; 10(6):585-8. PubMed ID: 3326892
[TBL] [Abstract][Full Text] [Related]
2. Glucocorticoid and partial mineralocorticoid deficiency associated with achalasia.
Lanes R; Plotnick LP; Bynum TE; Lee PA; Casella JF; Fox CE; Kowarski AA; Migeon CJ
J Clin Endocrinol Metab; 1980 Feb; 50(2):268-70. PubMed ID: 6243664
[TBL] [Abstract][Full Text] [Related]
3. Glomerulosa failure in congenital adrenocortical unresponsiveness to ACTH.
Davidai G; Kahana L; Hochberg Z
Clin Endocrinol (Oxf); 1984 May; 20(5):515-20. PubMed ID: 6378432
[TBL] [Abstract][Full Text] [Related]
4. [2 cases of congenital adrenocortical unresponsiveness to ACTH (author's transl)].
Kondo T; Ueda K; Murakami T
Nihon Naibunpi Gakkai Zasshi; 1980 Jun; 56(6):827-42. PubMed ID: 6250921
[TBL] [Abstract][Full Text] [Related]
5. Syndrome of congenital adrenocortical unresponsiveness to ACTH. Report of six patients.
Berberoğlu M; Aycan Z; Ocal G; Begeot M; Naville D; Akar N; Adiyaman P; Evliyaoglu O; Penhoat A
J Pediatr Endocrinol Metab; 2001; 14(8):1113-8. PubMed ID: 11592568
[TBL] [Abstract][Full Text] [Related]
6. Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency.
Chan LF; Metherell LA; Krude H; Ball C; O'Riordan SM; Costigan C; Lynch SA; Savage MO; Cavarzere P; Clark AJ
Clin Endocrinol (Oxf); 2009 Aug; 71(2):171-5. PubMed ID: 19170705
[TBL] [Abstract][Full Text] [Related]
7. Isolated deficiency of glucocorticoids presenting with cholestasis.
Berberoğlu M; Yiğit S; Ocal G; Kansu A; Tarcan A; Girgin N; Suskan E
Acta Paediatr Jpn; 1998 Aug; 40(4):378-80. PubMed ID: 9745786
[TBL] [Abstract][Full Text] [Related]
8. A novel mutation in the MC2R gene causing familial glucocorticoid deficiency type 1.
Akin MA; Akin L; Coban D; Ozturk MA; Bircan R; Kurtoglu S
Neonatology; 2011; 100(3):277-81. PubMed ID: 21701219
[TBL] [Abstract][Full Text] [Related]
9. Isolated glucocorticoid deficiency and ACTH receptor mutations.
Tsigos C
Arch Med Res; 1999; 30(6):475-80. PubMed ID: 10714360
[TBL] [Abstract][Full Text] [Related]
10. Familial glucocorticoid deficiency with a point mutation in the ACTH receptor: a case report.
Kim CJ; Woo YJ; Kim GH; Yoo HW
J Korean Med Sci; 2009 Oct; 24(5):979-81. PubMed ID: 19795005
[TBL] [Abstract][Full Text] [Related]
11. Familial glucocorticoid deficiency. Studies of diagnosis and pathogenesis.
Thistlethwaite D; Darling JA; Fraser R; Mason PA; Rees LH; Harkness RA
Arch Dis Child; 1975 Apr; 50(4):291-7. PubMed ID: 238474
[TBL] [Abstract][Full Text] [Related]
12. Bioinactive ACTH causing glucocorticoid deficiency.
Samuels ME; Gallo-Payet N; Pinard S; Hasselmann C; Magne F; Patry L; Chouinard L; Schwartzentruber J; René P; Sawyer N; Bouvier M; Djemli A; Delvin E; Huot C; Eugene D; Deal CL; Van Vliet G; Majewski J; Deladoëy J;
J Clin Endocrinol Metab; 2013 Feb; 98(2):736-42. PubMed ID: 23293326
[TBL] [Abstract][Full Text] [Related]
13. Isolated glucocorticoid insufficiency.
Werder EA; Haller R; Vetter W; Zachmann M; Siebenmann R
Helv Paediatr Acta; 1975 Jul; 30(2):175-83. PubMed ID: 1150481
[TBL] [Abstract][Full Text] [Related]
14. Isolated glucocorticoid deficiency: metabolic and endocrine studies in a 5-year-old boy.
Soltesz G; Dillon MJ; Jenkins PA; Moore A; Aynsley-Green A
Eur J Pediatr; 1985 Mar; 143(4):297-300. PubMed ID: 2985394
[TBL] [Abstract][Full Text] [Related]
15. Nonsalt-losing congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency with normal glomerulosa function.
Pang S; Levine LS; Stoner E; Opitz JM; Pollack MS; Dupont B; New MI
J Clin Endocrinol Metab; 1983 Apr; 56(4):808-18. PubMed ID: 6300166
[TBL] [Abstract][Full Text] [Related]
16. Sugar or salt? The relative roles of the glucocorticoid and mineralocorticoid axes in traumatic shock.
Nelson DW; Black GE; Thomas RL; Eckert MJ; Hoffer ZS; Martin MJ
J Trauma Acute Care Surg; 2015 Dec; 79(6):1023-9. PubMed ID: 26680140
[TBL] [Abstract][Full Text] [Related]
17. The use of theophylline as an in vivo probe of adrenocortical function.
Geffner ME; Lippe BM; Kaplan SA; Itami RM
J Clin Endocrinol Metab; 1982 Jul; 55(1):56-60. PubMed ID: 6281302
[TBL] [Abstract][Full Text] [Related]
18. Familial glucocorticoid deficiency presenting with hyperpigmentation, gigantism, and motor development delay: a case report.
Uyangoda K; Kamalanathan P; Mettananda S
J Med Case Rep; 2019 Sep; 13(1):280. PubMed ID: 31481085
[TBL] [Abstract][Full Text] [Related]
19. Effects of continued adrenocorticotropin stimulation on the mineralocorticoid hormones in classical and nonclassical simple virilizing types of 21-hydroxylase deficiency.
Kater CE; Biglieri EG; Wajchenberg B
J Clin Endocrinol Metab; 1985 Jun; 60(6):1057-62. PubMed ID: 2987285
[TBL] [Abstract][Full Text] [Related]
20. Adrenocorticotropin receptor gene mutations in familial glucocorticoid deficiency: relationships with clinical features in four families.
Weber A; Toppari J; Harvey RD; Klann RC; Shaw NJ; Ricker AT; Näntö-Salonen K; Bevan JS; Clark AJ
J Clin Endocrinol Metab; 1995 Jan; 80(1):65-71. PubMed ID: 7829641
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
